{{Rsnum
|rsid=13265018
|Gene=TNFRSF10B
|Chromosome=8
|position=23028507
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.1226
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TNFRSF10B
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 19.0 | 81.0
| HCB | 2.3 | 0.0 | 97.7
| JPT | 0.0 | 0.0 | 100.0
| YRI | 4.9 | 39.3 | 55.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.3 | 0.0 | 97.7
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=13265018
|allele=G
|frequency=0.893
|uid=1103652271759
|type=homozygous_SNP
|hugo=TNFRSF10B
|ensembl gene=ENSG00000120889
|ensembl transcript=ENST00000381063
|sift=TOLERATED
|disease=Defects in TNFRSF10B may be a cause of squamous cell carcinoma of the head and neck (HNSCC) (MIM:275355).
}}

{{GET Evidence
|gene=TNFRSF10B
|aa_change=Val191Ala
|aa_change_short=V191A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs13265018
|overall_frequency_n=9176
|overall_frequency_d=10758
|overall_frequency=0.852947
|n_genomes=55
|n_genomes_annotated=0
|n_haplomes=92
|n_articles=0
|n_articles_annotated=0
|nblosum100=2
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}